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Clinical outcomes with pemetrexed-based systemic therapies in RET-rearranged lung cancers.
Drilon, A; Bergagnini, I; Delasos, L; Sabari, J; Woo, K M; Plodkowski, A; Wang, L; Hellmann, M D; Joubert, P; Sima, C S; Smith, R; Somwar, R; Rekhtman, N; Ladanyi, M; Riely, G J; Kris, M G.
Afiliação
  • Drilon A; Department of Medicine drilona@mskcc.org.
  • Bergagnini I; Department of Medicine.
  • Delasos L; Department of Medicine.
  • Sabari J; Department of Medicine.
  • Woo KM; Department of Epidemiology/Biostatistics.
  • Plodkowski A; Department of Radiology.
  • Wang L; Department of Pathology, Memorial Sloan Kettering Cancer Center, New York, USA.
  • Hellmann MD; Department of Medicine.
  • Joubert P; Department of Pathology, Université Laval, Québec, Canada.
  • Sima CS; Department of Epidemiology/Biostatistics.
  • Smith R; Department of Pathology, Memorial Sloan Kettering Cancer Center, New York, USA.
  • Somwar R; Department of Pathology, Memorial Sloan Kettering Cancer Center, New York, USA.
  • Rekhtman N; Department of Pathology, Memorial Sloan Kettering Cancer Center, New York, USA.
  • Ladanyi M; Department of Pathology, Memorial Sloan Kettering Cancer Center, New York, USA.
  • Riely GJ; Department of Medicine.
  • Kris MG; Department of Medicine.
Ann Oncol ; 27(7): 1286-91, 2016 07.
Article em En | MEDLINE | ID: mdl-27056998
ABSTRACT

BACKGROUND:

RET rearrangements are targetable, oncogenic lung cancer drivers. While previous series have shown durable clinical benefit with pemetrexed-based therapies in ALK- and ROS1-rearranged lung cancers, the benefits of pemetrexed-based treatments in patients with RET-rearranged lung cancers relative to other genomic subsets have not previously been explored. PATIENTS AND

METHODS:

A retrospective review of patients with pathologically confirmed stage IIIB/IV lung adenocarcinomas and evidence of a RET, ROS1, or ALK rearrangement, or a KRAS mutation was conducted. Patients were eligible if they received treatment with pemetrexed alone or in combination. The primary outcome of progression-free survival (PFS), and secondary outcomes of overall response rate (ORR, RECIST v1.1), time to progression (TTP), and time to treatment discontinuation were compared between RET-rearranged and groups of ROS1-rearranged, ALK-rearranged, and KRAS-mutant lung cancers.

RESULTS:

We evaluated 104 patients. Patients with RET-rearranged lung cancers (n = 18) had a median PFS of 19 months [95% confidence interval (CI) 12-not reached (NR)] that was comparable with patients with ROS1- (23 months, 95% CI 14-NR, n = 10) and ALK-rearranged (19 months, 95% CI 15-36, n = 36) lung cancers, and significantly improved compared with patients with KRAS-mutant lung cancers (6 months, 95% CI 5-9, P < 0.001, n = 40). ORR (45%), median TTP (20 months, 95% CI 17-NR), and median time to treatment discontinuation (21 months, 95% CI 6-NR) in patients with RET-rearranged lung cancers were not significantly different compared with patients with ALK- and ROS1-rearranged lung cancers, and improved compared with patients with KRAS-mutant lung cancers.

CONCLUSION:

Durable benefits with pemetrexed-based therapies in RET-rearranged lung cancers are comparable with ALK- and ROS1-rearranged lung cancers. When selecting therapies for patients with RET-rearranged lung cancers, pemetrexed-containing regimens should be considered.
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Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Assunto principal: Proteínas Tirosina Quinases / Proteínas Proto-Oncogênicas / Receptores Proteína Tirosina Quinases / Carcinoma Pulmonar de Células não Pequenas / Proteínas Proto-Oncogênicas c-ret / Neoplasias Pulmonares Limite: Aged / Female / Humans / Male / Middle aged Idioma: En Revista: Ann Oncol Ano de publicação: 2016 Tipo de documento: Article

Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Assunto principal: Proteínas Tirosina Quinases / Proteínas Proto-Oncogênicas / Receptores Proteína Tirosina Quinases / Carcinoma Pulmonar de Células não Pequenas / Proteínas Proto-Oncogênicas c-ret / Neoplasias Pulmonares Limite: Aged / Female / Humans / Male / Middle aged Idioma: En Revista: Ann Oncol Ano de publicação: 2016 Tipo de documento: Article